Journal Article
- Intervention with kimchi microbial community ameliorates obesity by regulating gut microbiota
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Seong-Eun Park , Sun Jae Kwon , Kwang-Moon Cho , Seung-Ho Seo , Eun-Ju Kim , Tatsuya Unno , So-Hyeon Bok , Dae-Hun Park , Hong-Seok Son
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J. Microbiol. 2020;58(10):859-867. Published online September 2, 2020
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DOI: https://doi.org/10.1007/s12275-020-0266-2
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Abstract
- The objective of this study was to evaluate anti-obesity effects
of kimchi microbial community (KMC) on obesity and
gut microbiota using a high fat diet-induced mouse model
compared to effects of a single strain. Administration of KMC
decreased body weight, adipose tissue, and liver weight gains.
Relative content of Muribaculaceae in the gut of the KMCtreated
group was higher than that in the high-fat diet (HFD)
group whereas relative contents of Akkermansiaceae, Coriobacteriaceae,
and Erysipelotrichaceae were lower in KMCtreated
group. Metabolic profile of blood was found to change
differently according to the administration of KMC and a
single strain of Lactobacillus plantarum. Serum metabolites
significantly increased in the HFD group but decreased in
the KMC-treated group included arachidic acid, stearic acid,
fumaric acid, and glucose, suggesting that the administration
of KMC could influence energy metabolism. The main genus
in KMC was not detected in guts of mice in KMC-treated
group. Since the use of KMC has advantages in terms of
safety, it has potential to improve gut microbial community
for obese people.
Review
- [Minireivew]Microbial consortia including methanotrophs: some benefits of living together
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Rajendra Singh , Jaewon Ryu , Si Wouk Kim
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J. Microbiol. 2019;57(11):939-952. Published online October 28, 2019
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DOI: https://doi.org/10.1007/s12275-019-9328-8
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29
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Abstract
- With the progress of biotechnological research and improvements
made in bioprocessing with pure cultures, microbial
consortia have gained recognition for accomplishing biological
processes with improved effectiveness. Microbes are
indispensable tool in developing bioprocesses for the production
of bioenergy and biochemicals while utilizing renewable
resources due to technical, economic and environmental
advantages. They communicate with specific cohorts
in close proximity to promote metabolic cooperation. Use of
positive microbial associations has been recognized widely,
especially in food industries and bioremediation of toxic compounds
and waste materials. Role of microbial associations
in developing sustainable energy sources and substitutes for
conventional fuels is highly promising with many commercial
prospects. Detoxification of chemical contaminants sourced
from domestic, agricultural and industrial wastes has also been
achieved through microbial catalysis in pure and co-culture
systems. Methanotrophs, the sole biological sink of greenhouse
gas methane, catalyze the methane monooxygenasemediated
oxidation of methane to methanol, a high energy
density liquid and key platform chemical to produce commodity
chemical compounds and their derivatives. Constructed
microbial consortia have positive effects, such as improved
biomass, biocatalytic potential, stability etc. In a methanotroph-
heterotroph consortium, non-methanotrophs provide
key nutrient factors and alleviate the toxicity from the culture.
Non-methanotrophic organisms biologically stimulate the
growth and activity of methanotrophs via production of growth
stimulators. However, methanotrophs in association with cocultured
microorganisms are in need of further exploration
and thorough investigation to study their interaction mode
and application with improved effectiveness.
Journal Articles
- A novel methanotroph in the genus Methylomonas that contains a distinct clade of soluble methane monooxygenase
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Ngoc-Loi Nguyen , Woon-Jong Yu , Hye-Young Yang , Jong-Geol Kim , Man-Young Jung , Soo-Je Park , Seong-Woon Roh , Sung-Keun Rhee
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J. Microbiol. 2017;55(10):775-782. Published online September 28, 2017
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DOI: https://doi.org/10.1007/s12275-017-7317-3
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11
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22
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Abstract
- Aerobic methane oxidation is a key process in the global carbon
cycle that acts as a major sink of methane. In this study,
we describe a novel methanotroph designated EMGL16-1
that was isolated from a freshwater lake using the floating
filter culture technique. Based on a phylogenetic analysis of
16S rRNA gene sequences, the isolate was found to be closely
related to the genus Methylomonas in the family Methylococcaceae
of the class Gammaproteobacteria with 94.2–97.4%
16S rRNA gene similarity to Methylomonas type strains. Comparison
of chemotaxonomic and physiological properties
further suggested that strain EMGL16-1 was taxonomically
distinct from other species in the genus Methylomonas. The
isolate was versatile in utilizing nitrogen sources such as molecular
nitrogen, nitrate, nitrite, urea, and ammonium. The
genes coding for subunit of the particulate form methane
monooxygenase (pmoA), soluble methane monooxygenase
(mmoX), and methanol dehydrogenase (mxaF) were detected
in strain EMGL16-1. Phylogenetic analysis of mmoX indicated
that mmoX of strain EMGL16-1 is distinct from those
of other strains in the genus Methylomonas. This isolate probably
represents a novel species in the genus. Our study provides
new insights into the diversity of species in the genus
Methylomonas and their environmental adaptations.
- Metagenomic analysis reveals the contribution of anaerobic methanotroph-1b in the oxidation of methane at the Ulleung Basin, East Sea of Korea
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Jin-Woo Lee , Kae Kyoung Kwon , Jang-Jun Bahk , Dong-Hun Lee , Hyun Sook Lee , Sung Gyun Kang , Jung-Hyun Lee
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J. Microbiol. 2016;54(12):814-822. Published online November 26, 2016
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DOI: https://doi.org/10.1007/s12275-016-6379-y
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Abstract
- We have previously identified a sulfate methane transition
zone (SMTZ) within the methane hydrate-bearing sediment
in the Ulleung Basin, East Sea of Korea, and the presence of
ANME-1b group in the sediment has been shown by phylogenetic
analysis of a 16S rRNA gene. Herein, we describe
taxonomic and functional profiling in the SMTZ sample by
metagenomic analysis, comparing with that of surface sediment.
Metagenomic sequences of 115 Mbp and 252 Mbp
were obtained from SMTZ and surface sediments, respectively.
The taxonomic profiling using BLASTX against the
SEED within MG-RAST showed the prevalence of methanogens
(19.1%), such as Methanosarcinales (12.0%) and
Methanomicrobiales (4.1%) predominated within the SMTZ
metagenome. A number of 185,200 SMTZ reads (38.9%) and
438,484 surface reads (62.5%) were assigned to functional
categories, and methanogenesis-related reads were statistically
significantly overrepresented in the SMTZ metagenome.
However, the mapping analysis of metagenome reads to the
reference genomes, most of the sequences of the SMTZ metagenome
were mapped to ANME-1 draft genomes, rather
than those of methanogens. Furthermore, the two copies of
the methyl-coenzyme M reductase gene (mcrA) segments
of the SMTZ metagenome were clustered with ANME-1b in
the phylogenetic cluster. These results indicate that ANME-
1b reads were miss-annotated to methanogens due to limitation
of database. Many of key genes necessary for reverse
methanogenesis were present in the SMTZ metagenome,
except for N5,N10-methenyl-H4MPT reductase (mer) and CoBCoM
heterodisulfide reductase subunits D and E (hdrDE). These data suggest that the ANME-1b represents the primary
player the anaerobic methane oxidation in the SMTZ,
of the methane hydrate-bearing sediment at the Ulleung
Basin, East Sea of Korea.
Research Support, Non-U.S. Gov't
- Isolation and Taxonomic Characterization of a Novel Type I Methanotrophic Bacterium
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Hee Gon Kim , Gui Hwan Han , Chi-Yong Eom , Si Wouk Kim
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J. Microbiol. 2008;46(1):45-50.
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DOI: https://doi.org/10.1007/s12275-008-0017-2
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Abstract
- A methane-oxidizing bacterium was isolated from the effluent of manure and its molecular and biochemical properties were characterized. The isolate was aerobic, Gram-negative, and non-motile. The organism had a type I intracytoplasmic membrane structure and granular inclusion bodies. The outer cell wall surface (S-layers) was tightly packed with cup-shaped structures. Colonies were light yellow on nitrate mineral salt agar medium. In addition, the organism was catalase and oxidase positive. The isolate used the ribulose monophosphate (RuMP) pathway for carbon assimilation, and was able to utilize methane and methanol as a sole carbon and energy source, however, it could not utilize any other organic compounds that were tested. The cells grew well in a mixture of methane and air (methane:air=1:1, v/v) in a compulsory circulation diffusion system, and when grown under those conditions, the optimum pH was approximately 7.0 and the optimal temperature was 30°C. In addition, the specific growth rate and generation time were 0.13 per h and 5.43 h, respectively, when grown under the optimum conditions. The major ubiquinone was Q-8, and the G+C mol% of the DNA was 55.3. Phylogenetic analyses based on the 16S rRNA gene sequence comparisons showed that this bacterium belongs to a group of type I methanotrophs, and that it is most closely related to Methylomicrobium, with a sequence similarity of 99%. Therefore, the isolate was named Methylomicrobium sp. HG-1.